# K082667: Visionsense Stereoscopic Vision System (VS System)

- Pathway: 510(k) (Traditional)
- Applicant: Visionsense, Ltd.
- Decided: Oct 30, 2008 after 48 days
- Product code: EOB (Nasopharyngoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K874215 (1988). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081102: Vsu - Visionsense Stereoscopic Vision System, Visionsense, Ltd. (2008) Summary page 1.
- K073279: VS-Visionsense Stereoscopic Vision System, Visionsense, Ltd. (2008) Summary page 1.
- K032822: Asap Sinuscope 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0, Asap Endoscopic Products GmbH (2004) Summary page 1.

## Most influential descendants
- K162410: TIPCAM 1S 3D System (2017), 0 descendants of its own

## Indications for use
The VS,, is intended to visualize the nasal cavity and nasal pharynx during diagnostic and therapeutic procedures, as well as for viewing internal surgical sites during general surgical procedures and for use in visualization of ventricles and structures within the brain during neurological surgical procedures.

Source page: https://510kreport.com/device/K082667
Methodology: https://510kreport.com/methodology